Abstract

9Z, 11E, 13-TetradecatrienaI, a component of the sex pheromone of the carob moth, was synthesized by a short and efficient route, with a high degree of stereoselectivity. Key steps included the Pd-catalyzed construction of a conjugated dienynol intermediate from E-l, 2-dichloroethylene, and stereo- and regiospecific reduction of the dienynol with activated zinc in aqueous alcohol.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.